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American Journal of Medical Genetics
|
January 1, 1980
Oligohydramnios hampering prenatal diagnosis of Meckel syndrome
M Verjaal, A H Meyer, M J Becker-Bloemkolk, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
February 1, 1979
Prenatal diagnosis of congenital malformations in 500 pregnancies
N J Leschot, P E Treffers, M Verjaal, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
July 1, 1980
Severe congenital skin defects in a newborn. Case report and relevance of several obstetrical parameters
N J Leschot, P E Treffers, M J Becker-Bloemkolk, et al.
Clinical Genetics
|
September 1, 1979
Five familial cases with a trisomy 16p syndrome due to translocation
N J Leschot, J J De Nef, J P Geraedts, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1994
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia
M Mannens, J M Hoovers, E Redeker, et al.
British Medical Journal (Clinical Research Ed.)
|
August 15, 1987
Chorionic villi sampling: cytogenetic and clinical findings in 500 pregnancies
N J Leschot, H Wolf, M Verjaal, et al.
Clinical Genetics
|
September 1, 1990
An evaluation of 75 terminations of pregnancy based on abnormal laboratory findings at first trimester CVS
N J Leschot, H H Kanhai, C J van Asperen, et al.
British Journal of Obstetrics and Gynaecology
|
June 1, 1989
Cytogenetic findings in 1250 chorionic villus samples obtained in the first trimester with clinical follow-up of the first 1000 pregnancies
N J Leschot, H Wolf, A C Van Prooijen-Knegt, et al.
Prenatal Diagnosis
|
August 1, 1996
The outcome of pregnancies with confined placental chromosome mosaicism in cytotrophoblast cells
N J Leschot, G H Schuring-Blom, A C Van Prooijen-Knegt, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 29 results.
American Journal of Medical Genetics
|
January 1, 1980
Oligohydramnios hampering prenatal diagnosis of Meckel syndrome
M Verjaal, A H Meyer, M J Becker-Bloemkolk, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
February 1, 1979
Prenatal diagnosis of congenital malformations in 500 pregnancies
N J Leschot, P E Treffers, M Verjaal, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
July 1, 1980
Severe congenital skin defects in a newborn. Case report and relevance of several obstetrical parameters
N J Leschot, P E Treffers, M J Becker-Bloemkolk, et al.
Clinical Genetics
|
September 1, 1979
Five familial cases with a trisomy 16p syndrome due to translocation
N J Leschot, J J De Nef, J P Geraedts, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1994
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia
M Mannens, J M Hoovers, E Redeker, et al.
British Medical Journal (Clinical Research Ed.)
|
August 15, 1987
Chorionic villi sampling: cytogenetic and clinical findings in 500 pregnancies
N J Leschot, H Wolf, M Verjaal, et al.
Clinical Genetics
|
September 1, 1990
An evaluation of 75 terminations of pregnancy based on abnormal laboratory findings at first trimester CVS
N J Leschot, H H Kanhai, C J van Asperen, et al.
British Journal of Obstetrics and Gynaecology
|
June 1, 1989
Cytogenetic findings in 1250 chorionic villus samples obtained in the first trimester with clinical follow-up of the first 1000 pregnancies
N J Leschot, H Wolf, A C Van Prooijen-Knegt, et al.
Prenatal Diagnosis
|
August 1, 1996
The outcome of pregnancies with confined placental chromosome mosaicism in cytotrophoblast cells
N J Leschot, G H Schuring-Blom, A C Van Prooijen-Knegt, et al.
Page
of 3